510(k) K800817

SHIELD DISP. REINFORCED DRAPE SHEETS by American Convertors Div., American Pharmaseal — Product Code KKX

K800817 is an FDA 510(k) premarket notification submitted by American Convertors Div., American Pharmaseal for the device "SHIELD DISP. REINFORCED DRAPE SHEETS". The FDA issued a decision of Substantially Equivalent on May 2, 1980. The device falls under product code KKX (Drape, Surgical, Antimicrobial), a Class II device regulated under 21 CFR 878.4370. American Convertors Div., American Pharmaseal has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 2, 1980
Date Received
April 11, 1980
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drape, Surgical, Antimicrobial
Device Class
Class II
Regulation Number
878.4370
Review Panel
HO
Submission Type

Surgical drapes with an antimicrobial agent are subject to 510(k) review, under the procedures established by the 21st Century Cures Act. This product code is the class II non-exempt counterpart of PUI.